Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome-Reference-Cited by-同舟云学术

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Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome

Published:1990-07 Issue:3 Volume:7 Page:299-306
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Carey A.H.,Roach S.,Willamson R.,Dumanski J.P.,Nordenskiold M.,Collins V.P.,Rouleau G.,Blin N.,Jalbert P.,Scambler P.J.

Publisher

Elsevier BV

Subject

Genetics

Reference35 articles.

1. DiGeorge syndrome and 22q11 rearrangements;Augusseau;Hum. Genet,1986

2. Translocation involving chromosome 22 in Ewing's sarcoma;Aurias;Cancer Genet. Cytogenet,1984

3. Linear order of the four BCR-related loci in 22q11;Budarf;Genomics,1988

4. In situ hybridization and translocation breakpoint mapping;Cannizzaro;Cytogenet. Cell Genet,1985

5. The spectrum of the DiGeorge syndrome;Conley;J. Pediatr,1979

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4. The spectrum of parathyroid gland dysfunction associated with the microdeletion 22q11;European Journal of Endocrinology;2006-07

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